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FDA 510(k)

AQUEOUS BLOOD GAS CONTROLS

K-Number: K812553 · 1981-09-23

ApplicantFisher Scientific Co., LLC
Decision Date1981-09-23
Product CodeJJS
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

AQUEOUS BLOOD GAS CONTROLS is the device name listed in this FDA 510(k) record. The listed applicant is Fisher Scientific Co., LLC. It received FDA 510(k) clearance on 1981-09-23 under 510(k) number K812553. The device is classified under product code JJS. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the AQUEOUS BLOOD GAS CONTROLS?

AQUEOUS BLOOD GAS CONTROLS is a medical device that received FDA 510(k) clearance on 1981-09-23. The listed applicant is Fisher Scientific Co., LLC. The 510(k) number is K812553.

When did AQUEOUS BLOOD GAS CONTROLS receive FDA 510(k) clearance?

AQUEOUS BLOOD GAS CONTROLS received FDA 510(k) clearance on 1981-09-23, under 510(k) number K812553.

Who is the listed applicant for AQUEOUS BLOOD GAS CONTROLS?

The FDA 510(k) record lists Fisher Scientific Co., LLC as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for AQUEOUS BLOOD GAS CONTROLS?

The FDA product code for AQUEOUS BLOOD GAS CONTROLS is JJS.

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Other records listing Fisher Scientific Co., LLC as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K930415MICROHEMATOCRIT ROTORK915825MARATHON 6K GENERAL-PURPOSE CENTRIFUGEK915441MARATHON 13K/H MICROHEMATOCRIT CENTRIFUGEK890534MODIFIED URIQUAL(TM) URINALYSIS CONTROL LEVEL 1K881275URIQUAL(TM) URINALYSIS CONTROLS (HUMAN) I & IIK874054FISHER DIAGNOSTICS HEMATALL III LAS REAGENT

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Related Devices (Code: JJS)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K152553CueSee HypoxicEurotrol B.V.K130415HIGH METABOLITE QUALICHECKRadiometer Medical ApsK130236RANGE + QUALICHECK LEVEL 1, RANGE + QUALICHECK LEVEL 2, RANGE + QUALICHECK LEVEL 3Radiometer Medical ApsK033063MISSION CONTROLSDiamond Diagnostics, Inc.K022525LIQUICHEK BLOOD GAS PLUS CO-OXIMETER CONTROL (RADIOMETER 700 SERIES) LEVELS, 1,2 AND 3, MODEL 507, 508, 509Bio-RadK022529LIQUICHEK BLOOD GAS PLUS CO-OXIMETER CONTROL (IL SYNTHESIS SERIES) LEVELS 1,2, AND 3, MODELS 667,668,669Bio-Rad

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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